CN1127254A - 新的1,3-二氢-2H-吡咯并[2,3-b]吡啶-2-酮和噁唑并[4,5-b]吡啶-2(3H)-酮化合物,它们的制备方法以及含有它们的药物组合物 - Google Patents

新的1,3-二氢-2H-吡咯并[2,3-b]吡啶-2-酮和噁唑并[4,5-b]吡啶-2(3H)-酮化合物,它们的制备方法以及含有它们的药物组合物 Download PDF

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Publication number
CN1127254A
CN1127254A CN95109180A CN95109180A CN1127254A CN 1127254 A CN1127254 A CN 1127254A CN 95109180 A CN95109180 A CN 95109180A CN 95109180 A CN95109180 A CN 95109180A CN 1127254 A CN1127254 A CN 1127254A
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CN
China
Prior art keywords
compound
pyridine
ketone
formula
methyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN95109180A
Other languages
English (en)
Chinese (zh)
Inventor
G·古勒梅
M·C·瓦尤德
L·萨维龙
P·帕维利
P·雷纳德
B·佩弗
D·H·卡格纳德
J·G·比佐-埃斯泼德
G·亚当
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ADIR SARL
Original Assignee
ADIR SARL
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from FR9408419A external-priority patent/FR2722196B1/fr
Priority claimed from FR9408418A external-priority patent/FR2722195B1/fr
Application filed by ADIR SARL filed Critical ADIR SARL
Publication of CN1127254A publication Critical patent/CN1127254A/zh
Pending legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pain & Pain Management (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Biomedical Technology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
CN95109180A 1994-07-07 1995-07-07 新的1,3-二氢-2H-吡咯并[2,3-b]吡啶-2-酮和噁唑并[4,5-b]吡啶-2(3H)-酮化合物,它们的制备方法以及含有它们的药物组合物 Pending CN1127254A (zh)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
FR9408419A FR2722196B1 (fr) 1994-07-07 1994-07-07 Nouveaux derives amines de 1,3-dihydro-2h-pyrrolo(2,3-b) pyridin-2-ones et oxazolo(4,5-b) pyridin-2 (3h)-ones, leur procede de preparation et les compositions pharmaceutique qui les contiennent
FR9408418 1994-07-07
FR9408419 1994-07-07
FR9408418A FR2722195B1 (fr) 1994-07-07 1994-07-07 Nouveaux derives de 1,3-dihydro-2h-pyrrolo(2,3-b) pyridin-2-ones et oxazolo(4,5-b) pyridin-2(3h)-ones, leur procede de preparation et les compositions pharmaceutiques qui les contiennent

Publications (1)

Publication Number Publication Date
CN1127254A true CN1127254A (zh) 1996-07-24

Family

ID=26231276

Family Applications (1)

Application Number Title Priority Date Filing Date
CN95109180A Pending CN1127254A (zh) 1994-07-07 1995-07-07 新的1,3-二氢-2H-吡咯并[2,3-b]吡啶-2-酮和噁唑并[4,5-b]吡啶-2(3H)-酮化合物,它们的制备方法以及含有它们的药物组合物

Country Status (9)

Country Link
US (2) US5618819A (sv)
EP (1) EP0691339A1 (sv)
JP (1) JPH0853447A (sv)
CN (1) CN1127254A (sv)
AU (1) AU683167B2 (sv)
CA (1) CA2153294A1 (sv)
FI (1) FI953327A (sv)
NO (1) NO952677L (sv)
NZ (1) NZ272516A (sv)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20140206893A1 (en) * 2011-09-01 2014-07-24 Dsm Ip Assets B.V. Process for the alkoxycarbonylation of functionalized alkenes

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US5618819A (en) * 1994-07-07 1997-04-08 Adir Et Compagnie 1,3-dihydro-2H-pyrrolo[2,3-b]pyridin-2-one and oxazolo[4,5-b]pyridin-2-(3H)-one compounds
US6166274A (en) * 1999-12-15 2000-12-26 Atofina Chemicals, Inc. Catalyzed liquid phase fluorination of 1230za
JP4953457B2 (ja) * 2004-10-27 2012-06-13 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ プロゲステロン受容体モジュレーターとしてのピリジンイミダゾール及びアザ−インドール
DE102005007694A1 (de) * 2005-02-18 2006-09-21 Henkel Kgaa Mittel zum Färben von keratinhaltigen Fasern
MY145694A (en) * 2005-04-11 2012-03-30 Xenon Pharmaceuticals Inc Spiroheterocyclic compounds and their uses as therapeutic agents
MY144968A (en) * 2005-04-11 2011-11-30 Xenon Pharmaceuticals Inc Spiro-oxindole compounds and their uses as therapeutic agents
AR053713A1 (es) * 2005-04-20 2007-05-16 Xenon Pharmaceuticals Inc Compuestos heterociclicos y sus usos como agentes terapeuticos
EP2865381A1 (en) * 2006-05-18 2015-04-29 Pharmacyclics, Inc. ITK inhibitors for treating blood cell malignancies
US20110294842A9 (en) * 2006-10-12 2011-12-01 Xenon Pharmaceuticals Inc. Spiro (furo [3, 2-c] pyridine-3-3' -indol) -2' (1'h)-one derivatives and related compounds for the treatment of sodium-channel mediated diseases, such as pain
US20110237567A9 (en) * 2006-10-12 2011-09-29 Xenon Pharmaceuticals Inc. Tricyclic spiro-oxindole derivatives and their uses as therapeutic agents
EP2073806B1 (en) * 2006-10-12 2012-02-15 Xenon Pharmaceuticals Inc. Use of spiro-oxindole compounds as therapeutic agents
EP2184272A4 (en) * 2007-08-21 2011-11-09 Shionogi & Co PIPERAZINE DERIVATIVE
EP2350091B1 (en) * 2008-10-17 2015-06-03 Xenon Pharmaceuticals Inc. Spiro-oxindole compounds and their use as therapeutic agents
CN106928247A (zh) 2008-10-17 2017-07-07 泽农医药公司 螺羟吲哚化合物及其作为治疗剂的用途
US8877772B2 (en) 2008-11-25 2014-11-04 University Of Rochester Substituted pyrrolo[2,3-B]pyridines as MLK inhibitors
AR077252A1 (es) 2009-06-29 2011-08-10 Xenon Pharmaceuticals Inc Enantiomeros de compuestos de espirooxindol y sus usos como agentes terapeuticos
PE20170202A1 (es) 2009-10-14 2017-03-24 Xenon Pharmaceuticals Inc Metodos sinteticos para compuestos espiro-oxoindol
US20110086899A1 (en) * 2009-10-14 2011-04-14 Xenon Pharmaceuticals Inc. Pharmaceutical compositions for oral administration
MA34083B1 (fr) 2010-02-26 2013-03-05 Xenon Pharmaceuticals Inc Compositions pharmaceutques de composé spiro-oxindole pour administration topique et leur utilisation en tant qu'agents thérapeutiques
NZ603644A (en) 2010-05-24 2014-10-31 Univ Rochester Bicyclic heteroaryl kinase inhibitors and methods of use
BR112013028895A2 (pt) 2011-05-10 2016-08-09 Bayer Ip Gmbh (tio)carbonilamidinas bicíclicas
CN104884059B (zh) 2012-11-30 2018-08-10 罗切斯特大学 用于hiv/aids治疗的混合谱系激酶抑制剂
MA41169A (fr) * 2014-12-17 2017-10-24 Acraf Composés antibactériens à large spectre d'activité
US9682033B2 (en) 2015-02-05 2017-06-20 Teva Pharmaceuticals International Gmbh Methods of treating postherpetic neuralgia with a topical formulation of a spiro-oxindole compound

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2244507A1 (en) * 1973-06-26 1975-04-18 Inst Nat Sante Rech Med Chalcones and analogues - analgesics having low toxicity
US4038396A (en) * 1975-02-24 1977-07-26 Merck & Co., Inc. Anti-inflammatory oxazole[4,5-b]pyridines
JPS6015635B2 (ja) * 1976-05-28 1985-04-20 久光製薬株式会社 新規なオキサゾロ〔4,5−b〕ピリジン誘導体
US4866074A (en) * 1987-05-08 1989-09-12 Rorer Pharmaceutical Corporation Naphtheridinone- and pyridooxazinone-pyridone compounds, cardiotonic compositions including same, and their uses
FR2650591B1 (fr) * 1989-08-07 1991-11-15 Science Organisation Nouveaux derives d'oxazolo pyridines, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
FR2652085A1 (fr) * 1989-09-20 1991-03-22 Science Organisation Nouveau procede de synthese de derives d'oxazolopyridines.
WO1991009598A1 (en) * 1990-01-05 1991-07-11 Pfizer Inc. Azaoxindole derivatives
FR2663929A1 (fr) * 1990-06-29 1992-01-03 Adir Nouveaux derives d'oxazolo pyridines, leur procede de preparation et les compositions pharmaceutiques qui les contiennent.
FR2669336B1 (fr) * 1990-11-20 1993-01-22 Adir Nouveaux derives d'oxazolo pyridines, leurs procedes de preparation et les compositions pharmaceutiques qui les contiennent.
US5618819A (en) * 1994-07-07 1997-04-08 Adir Et Compagnie 1,3-dihydro-2H-pyrrolo[2,3-b]pyridin-2-one and oxazolo[4,5-b]pyridin-2-(3H)-one compounds

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20140206893A1 (en) * 2011-09-01 2014-07-24 Dsm Ip Assets B.V. Process for the alkoxycarbonylation of functionalized alkenes
US9056829B2 (en) * 2011-09-01 2015-06-16 Dsm Ip Assets B.V. Process for the alkoxycarbonylation of functionalized alkenes

Also Published As

Publication number Publication date
NO952677L (no) 1996-01-08
US5618819A (en) 1997-04-08
AU2482795A (en) 1996-01-18
NZ272516A (en) 1996-10-28
JPH0853447A (ja) 1996-02-27
NO952677D0 (no) 1995-07-06
AU683167B2 (en) 1997-10-30
US5767128A (en) 1998-06-16
FI953327A0 (sv) 1995-07-06
EP0691339A1 (fr) 1996-01-10
FI953327A (sv) 1996-01-08
CA2153294A1 (fr) 1996-01-08

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